R&D Scientist – Analytical Development

Are you an experienced scientist that is lookig for a new challenge? Do you have experience in GMP and analytical chemistry?
If yes you might be the one we are looking for!

This is a consultant assignment with an initial duration of 9 months at our customer in Helsingborg. During the assignment you will be hired byt QRIOS!
We look forward receiving your application as soon as possible.

About the position
The analytical scientist will work within the Analytical Life Cycle Management section and support marketed OTC products primarily within EMEA/APAC but also globally. You will be in a regional team of 7 analytical colleagues.
Together with your colleagues you will provide analytical support for a series of projects associated with the currently marketed OTC products. Technical support will include but not be limited to; analytical support to product development, test method development and improvement, test method validation as well as test method transfers. Most of the laboratory work is performed using analytical techniques such as UPLC, HPLC and GC. The technical support will also include desktop related work such as performing and reporting analytical test method gap assessments


Responsibilities
• Laboratory work including development support, method development and improvement, validation and transfers
• Performing and reporting analytical gap assessments
• Collaborate with local R&D stakeholders such as Product Design, QA, Franchise, Regulatory, CMC and others to ensure flawless completion of the activities.

Your profile
• Minimum of BSc within a relevant chemistry or pharmaceutical area
• A minimum of 5 years in an analytical laboratory role supporting pharmaceutical manufacturing or product development with a major emphasis on product testing with analytical method development, optimization, validation, verification, transfer skills as an added bonus.
• Experience and deep knowledge with the chromatography system Empower as well as HPLC/UPLC, GC, dissolution and other major analytical techniques
• Comprehensive understanding of quality and regulatory compliance knowledge, pharmacopeia including USP, EP, ICH/WHO guidelines and good understanding of GMP systems
• Technical writing and documentation review abilities
• You need to be an innovative and a creative problem solver who can work independently, while managing multiple priorities successfully. Strong written and oral communication skills (English) are essential.
• Hands on experience from working in a GMP laboratory


About the organisation
Qrios Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at Qrios gives you opportunities to try different industries, companies and roles. Read more about how it is to be a consultant through us: https://www.qrios.se/karriar/tips/konsult/.

It suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.